Canonical Allele Identifier: CA1246139638
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022855T= , CM000664.2:g.39022855T= GRCh38
NC_000002.11:g.39249996T= , CM000664.1:g.39249996T= GRCh37
NC_000002.10:g.39103500T= NCBI36
NG_007530.1:g.102609A= , LRG_754:g.102609A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1453A=
ENST00000685279.1:c.340A= ENSP00000509424.1:p.Ile114=
ENST00000688043.1:n.1794A=
ENST00000689668.1:n.1580A=
ENST00000690876.1:c.1462A= ENSP00000508955.1:p.Ile488=
ENST00000691229.1:c.1462A= ENSP00000510437.1:p.Ile488=
ENST00000692089.1:c.1462A= ENSP00000508626.1:p.Ile488=
ENST00000692620.1:c.340A= ENSP00000509311.1:p.Ile114=
ENST00000402219.8:c.1573A= MANE Select ENSP00000384675.2:p.Ile525=
ENST00000395038.6:c.1573A= ENSP00000378479.2:p.Ile525=
ENST00000402219.6:c.1573A= ENSP00000384675.2:p.Ile525=
ENST00000426016.5:c.1573A= ENSP00000387784.1:p.Ile525=
NM_005633.3:c.1573A= , LRG_754t1:c.1573A= NP_005624.2:p.Ile525=
XM_005264515.3:c.1573A= XP_005264572.1:p.Ile525=
XM_011533060.1:c.1666A= XP_011531362.1:p.Ile556=
XM_011533061.1:c.1666A= XP_011531363.1:p.Ile556=
XM_011533062.1:c.1552A= XP_011531364.1:p.Ile518=
XM_011533063.1:c.1549A= XP_011531365.1:p.Ile517=
XM_011533064.1:c.1402A= XP_011531366.1:p.Ile468=
XM_011533065.1:c.1666A= XP_011531367.1:p.Ile556=
XM_011533066.1:c.508A= XP_011531368.1:p.Ile170=
XM_005264515.4:c.1573A= XP_005264572.1:p.Ile525=
XM_011533062.2:c.1552A= XP_011531364.1:p.Ile518=
XM_011533064.2:c.1402A= XP_011531366.1:p.Ile468=
NM_001382394.1:c.1552A= NP_001369323.1:p.Ile518=
NM_001382395.1:c.1573A= NP_001369324.1:p.Ile525=
NM_005633.4:c.1573A= MANE Select NP_005624.2:p.Ile525=
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